Zhang Mei-bian, Jin Li-fen, He Ji-liang, Hu Jun, Zheng Wei
Institute of Environmental and Occupational Health, Medical School of Zhejiang University, Hangzhou 310006, China.
Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2003 Aug;21(4):266-9.
To study the combined damage-effects of low-intensity 2,450 MHz microwave (MW) with three chemical mutagens on human lymphocyte DNA.
DNA damage of lymphocytes exposed to microwave and(or) with chemical mutagens were observed at different incubation time (0 h or 21 h) with comet assay in vitro. Three combination-exposure ways of MW with chemicals were used: MW irradiation before chemical exposures, simultaneously exposed to MW and chemicals and MW irradiation after chemical exposures. The three chemical mutagens were mitomycin C (MMC, DNA crosslinker), bleomycin (BLM, radiometric agent), methyl methanesulfonate (MMS, alkylating agent). The exposure time of MW and chemical mutagens were 2 h and 3 h respectively.
The differences of comet tail length between MW group and control group were not significant when lymphocytes were incubated for 0 h or 21 h (P > 0.05). However, when lymphocytes were incubated for 21 h with 30.00 micro mol/L of MMC, the comet tail lengths of MW + MMC group, MW-MMC group and MMC + MW group were (18.00 +/- 5.96), (21.79 +/- 11.47) and (22.32 +/- 8.10) micro m respectively; while with 3.00 micro mol/L of MMC, the comet tail lengths were (8.99 +/- 3.75), (12.40 +/- 5.35) and (14.00 +/- 5.38) micro m respectively, which were significantly higher than those of corresponding MMC groups [(9.42 +/- 3.34) and (6.50 +/- 2.89) micro m, P < 0.01 or P < 0.05]. The DNA damage of MW plus BLM groups and MW plus MMS groups were not significantly different from the corresponding BLM and MMS groups (P < 0.05).
2 450 MHz MW (5 mW/cm(2)) did not induce DNA damage directly, but could enhance the DNA damage effects induced by MMC. The synergistic effects of 2 450 MHz MW with BLM and MMS were not obvious.
研究低强度2450兆赫微波(MW)与三种化学诱变剂对人淋巴细胞DNA的联合损伤效应。
采用体外彗星试验,观察在不同孵育时间(0小时或21小时)下,暴露于微波和(或)化学诱变剂的淋巴细胞的DNA损伤情况。采用微波与化学物质的三种联合暴露方式:化学物质暴露前进行微波照射、同时暴露于微波和化学物质、化学物质暴露后进行微波照射。三种化学诱变剂分别为丝裂霉素C(MMC,DNA交联剂)、博来霉素(BLM,辐射计量剂)、甲基磺酸甲酯(MMS,烷化剂)。微波和化学诱变剂的暴露时间分别为2小时和3小时。
当淋巴细胞孵育0小时或21小时时,微波组与对照组之间的彗星尾长差异不显著(P>0.05)。然而,当淋巴细胞与30.00微摩尔/升的MMC孵育21小时时,MW+MMC组、MW-MMC组和MMC+MW组的彗星尾长分别为(18.00±5.96)、(21.79±11.47)和(22.32±8.10)微米;而与3.00微摩尔/升的MMC孵育时,彗星尾长分别为(8.99±3.75)、(12.40±5.35)和(14.00±5.38)微米,均显著高于相应MMC组的彗星尾长[(9.42±3.34)和(6.50±2.89)微米,P<0.01或P<0.05]。MW加BLM组和MW加MMS组的DNA损伤与相应的BLM和MMS组无显著差异(P<0.05)。
2450兆赫微波(5毫瓦/平方厘米)不能直接诱导DNA损伤,但可增强MMC诱导的DNA损伤效应。2450兆赫微波与BLM和MMS的协同效应不明显。